Technology Process of (E)-4-(3-benzoyl-1H-pyrrol-1-yl)-2-hydroxybenzaldoxime
There total 4 articles about (E)-4-(3-benzoyl-1H-pyrrol-1-yl)-2-hydroxybenzaldoxime which
guide to synthetic route it.
The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:
synthetic route:
- Guidance literature:
-
With
hydroxylamine hydrochloride;
In
ethanol; water;
at 50 ℃;
for 1h;
Inert atmosphere;
DOI:10.1016/j.bmc.2014.02.016
- Guidance literature:
-
Multi-step reaction with 3 steps
1: sodium hydroxide; water / 1,4-dioxane / 20 °C / Inert atmosphere
2: magnesium chloride; triethylamine; sodium; phosphorus pentoxide; calcium hydride / acetonitrile / 72 h / Reflux; Inert atmosphere; Molecular sieve
3: hydroxylamine hydrochloride / water; ethanol / 1 h / 50 °C / Inert atmosphere
With
calcium hydride; phosphorus pentoxide; hydroxylamine hydrochloride; water; sodium; triethylamine; sodium hydroxide; magnesium chloride;
In
1,4-dioxane; ethanol; water; acetonitrile;
DOI:10.1016/j.bmc.2014.02.016
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: aluminum (III) chloride / 1,2-dichloro-ethane / 0.25 h / 20 °C / Inert atmosphere
1.2: 48 h / 20 °C / Inert atmosphere
2.1: sodium hydroxide; water / 1,4-dioxane / 20 °C / Inert atmosphere
3.1: magnesium chloride; triethylamine; sodium; phosphorus pentoxide; calcium hydride / acetonitrile / 72 h / Reflux; Inert atmosphere; Molecular sieve
4.1: hydroxylamine hydrochloride / water; ethanol / 1 h / 50 °C / Inert atmosphere
With
aluminum (III) chloride; calcium hydride; phosphorus pentoxide; hydroxylamine hydrochloride; water; sodium; triethylamine; sodium hydroxide; magnesium chloride;
In
1,4-dioxane; ethanol; water; 1,2-dichloro-ethane; acetonitrile;
1.1: |Friedel-Crafts Acylation / 1.2: |Friedel-Crafts Acylation;
DOI:10.1016/j.bmc.2014.02.016